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A possible mechanism for the formation of ¢ó from I in ethyl alcohol is that ¢ò is first formed. Since I1 is soluble in dry ethyl alcohol to the extent of 0.5% at reflux temperature, it could react with the hydrogen sulfide to give the postulated intermediate addition product ¢ô. ¢ô would then break down under the reaction conditions to give the observed ¢ó and ethyl thionoacetate (¢õ). This proposed mechanism was tested by treating ¢ò with hydrogen sulfide in et'hyl alcohol. ¢ó, and dithiomalonamide[3,4] (¢ö) were identified in the product. ¢õ was identified by gas chroma ¢ò + H2S + C2H5OH + ¢ó + ¢õ + CH2(CSNH2)2 tography and by mass spectrometry. Further evidence for the identity of V was obtained by synthesis of ethyl thionoacetate from ethyl acetimidate and hydrogen sulfide.[5] This authentic sample was found to have the same retention time on the gas chromatographic column as ¢õ, and the mass spectrum obtqined on this sample was also identical with that of ¢õ. Other products identified by gas chromatography from the reaction of ¢ò with hydrogen sulfide in alcohol were hydrogen sulfide, ethyl alcohol, and small quantities of ethyl acetate. The ethyl acetate probably resulted from hydrolysis or from oxidative exchange of the ethyl thionoacetate with air since thiono esters are noted for the ease with which the sulfur atom is removed.6 In some preparations, sulfur was isolated. It was also demonstrated by infrared and gas chromatographic analyses that ethyl thionoacetate is converted in the presence of air to ethyl acetate. |
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